Impact of Phellinus Gilvus Mycelia on Growth, Immunity and Fecal Microbiota in Weaned Piglets

Impact of Phellinus gilvus mycelia on growth, immunity and fecal microbiota in weaned piglets

Yuqing Sun1, Shi Zhong1, Bo Deng2, Qinsheng Jin3, Jie Wu2, Jinxi Huo1, Jianxun Zhu1, Cheng Zhang4 and Yougui Li1

1 Sericultural Research Institute, Zhejiang Academy of Agricultural Science, Hangzhou, China 2 Institute of Animal Husbandry and Veterinary Science, Zhejiang Academy of Agricultural Sciences, Hangzhou, China 3 Agricultural Technology Extension Service Center of Nanxun District, Huzhou, Zhejiang, China 4 Hangzhou Zhengxing Animal Husbandry co. LTD, Linan, Zhejiang, China

ABSTRACT Background. Antibiotics are the most commonly used growth-promoting additives in pig feed especially for weaned piglets. But in recent years their use has been restricted because of bacterial resistance. Phellinus, a genus of medicinal fungi, is widely used in Asia to treat gastroenteric dysfunction, hemrrhage, and tumors. Phellinus is reported to improve body weight on mice with colitis. Therefore, we hypothesize that it could benefit the health and growth of piglets, and could be used as an alternative to antibiotic. Here, the effect of Phellinus gilvus mycelia (SH) and antibiotic growth promoter (ATB) were investigated on weaned piglets. Methods. A total of 72 crossbred piglets were randomly assigned to three dietary treatment groups (n = 4 pens per treatment group with six piglets per pen). The control group was fed basal diet; the SH treatment group was fed basal diet containing 5 g/kg SH; the ATB treatment group was feed basal diet containing 75 mg/kg aureomycin and 20 mg/kg kitasamycin. The experiment period was 28 days. Average daily gain (ADG), average daily feed intake (ADFI), and feed intake to gain ratio were calculated. The concentrations of immunoglobulin G (IgG), interleukin-1β (IL-1β), tumor necrosis factor (TNF)-α and myeloperoxidase (MPO) in serum were assessed. Viable plate Submitted 22 January 2020 counts of Escherichia coli in feces were measured. Fecal microbiota was analyzed via Accepted 5 April 2020 Published 28 April 2020 the 16S rRNA gene sequencing method. Results. The ADG (1–28 day) of piglets was significantly higher in SH and ATB Corresponding author Yougui Li, [email protected] treatment groups (P < 0.05) compared to the control, and the ADG did not show significant difference between SH and ATB treatment groups (P > 0.05). Both SH and Academic editor β α Pedro Silva ATB treatments increased the MPO, IL-1 , and TNF- levels in serum compared to the control (P < 0.05), but the levels in SH group were all significantly higher than in the Additional Information and Declarations can be found on ATB group (P < 0.05). Fecal microbiological analysis showed that viable E. coli counts page 13 were dramatically decreased by SH and ATB. The 16S rRNA gene sequencing analysis DOI 10.7717/peerj.9067 showed that ATB shifted the microbiota structure drastically, and significantly increased the relative abundance of Prevotella, Megasphaera, and Faecalibacterium genera. But SH Copyright slightly influenced the microbiota structure, and only increased the relative abundance 2020 Sun et al. of Alloprevotella genus. Distributed under Conclusion. Our work demonstrated that though SH slightly influenced the microbiota Creative Commons CC-BY 4.0 structure, it markedly reduced the fecal E. coli population, and improved growth and OPEN ACCESS

How to cite this article Sun Y, Zhong S, Deng B, Jin Q, Wu J, Huo J, Zhu J, Zhang C, Li Y. 2020. Impact of Phellinus gilvus mycelia on growth, immunity and fecal microbiota in weaned piglets. PeerJ 8:e9067 http://doi.org/10.7717/peerj.9067 innate immunity in piglets. Our finding suggested that SH could be an alternative to ATB in piglet feed.

Subjects Agricultural Science, Biotechnology, Microbiology, Veterinary Medicine, Zoology Keywords Growth promoting, Piglet, Phellinus gilvus, Fecal microbiota, Immunological parameters, Antibiotic

INTRODUCTION Antibiotics have been used as feed additives in livestock and poultry for decades, but their use has been restricted because of the speculated risk of generating antibiotic resistance in pathogenic bacteria, especially since the European Union banned their use in food- producing animals in 2006 (Castanon, 2007). Consequently, many alternatives have been applied to control or prevent clinical diseases and maximize growth performance. For example, traditional Chinese medicines, which have been widely used in China to treat various diseases and conditions, became important sources of functional feed additives (Liu, Tong & Zhou, 2011). Many Chinese medicines are demonstrated to be effective in promoting health and growth in livestock (Song et al., 2010; Hong et al., 2012). The Phellinus mushroom, which is called Sanghuang in Chinese, is a genus of basidiomycetous fungi belonging to Hymenochaetaceae. Phellinus spp. has been widely used in Asian countries to treat gastroenteric dysfunction, hemorrhage, and tumors (Song et al., 2008; Chen et al., 2016). The immunity-modulating, anti-inflammatory, and antitumor effects of Phellinus spp. are well documented (Zhou et al., 2014; Suabjakyong et al., 2015; Gao et al., 2017; Wang et al., 2017). In our previous study, the extract of Phellinus ameliorated intestinal injury and improved the body weight of mice with colitis (Sun et al., 2018). However, little is known about the effect of Phellinus on livestock. Therefore, the present research aimed to investigate whether Phellinus could promote growth and health of piglets and be an alternative to antibiotic growth promoter (ATB) in feed. Gut microbiota plays an important role in the digestion, fermentation, and metabolism of many chemical compounds in food (Feng, Chen & Wang, 2018). The bioactivities of functional foods and drugs, such as cranberry (Anhe et al., 2015), ganoderma (Chang et al., 2015), and metformin (Shin et al., 2014), are also actively mediated by the gut microbiota. Therefore, the gut microbiota is a potential target for nutrition intervention to maintain animal health. In this study, the effect of Phellinus gilvus mycelia (SH) on the growth parameters and immunological parameters of weaned piglets was compared with that of ATB. The effects of SH and ATB on the fecal microbiota were also investigated. Our work demonstrated that SH was comparable to ATB in promoting growth of piglets, and it was more effective than ATB in enhancing innate immunity. SH markedly decreased fecal viable Escherichia coli counts as ATB did. But unlike ATB, which altered microbiota structure greatly, SH slightly influenced the structure of microbiota.

Sun et al. (2020), PeerJ, DOI 10.7717/peerj.9067 2/18 MATERIALS & METHODS Preparation of P. gilvus mycelia (SH) P. gilvus strain (preserved at the Sericultural Research Institute, Zhejiang Academy of Agricultural Science, Hangzhou, China) was incubated in sterile liquid culture medium (ingredients are provided in Table S1) in a fermentation tank at 25 ◦C with stirring speed of 100 r/min. The entire culture process was sterile. After 2 weeks, the mycelia of P. gilvus growing in the fermentation tank was separated from the liquid culture medium with a filter and dried at 65 ◦C. The dried mycelia were then ground into fine powder and stored at −20 ◦C before use. The SH was tested to have 39.8% crude protein, 15.2% crude fiber, 11.1% crude fat, 4.3% ash, 7.5% water-soluble polysaccharide, and 2.5% polyphenol. Experimental design The experiment was conducted in Hangzhou Zhengxing Animal Husbandry co. LTD (Linan, Zhejiang, China), and all the piglets used in this experiment were from this company. The trial was approved by the farm’s veterinary consultant, and all procedures were compliant with Chinese regulations and were approved by the Medical Ethics Committee of Zhejiang Academy of Agricultural Sciences (No. 2017-050). A total of 72 crossbred piglets [Duroc × (Landrace × Large White), 7.51 ± 0.88 kg BW, 36 barrows and 36 gilts] weaned at 28 d of age were used in a 28-day feeding trial. The piglets were assigned to three dietary treatment groups with four replicate pens per treatment and six piglets (three barrows and three gilts) per pen. Each pen was equipped with a self-feeder and a nipple waterer. Piglets had free access to water and diets. A combination of daylight and artificial light was used, and room temperature was controlled at 24−26 ◦C. The treatments included basal diet without antibiotics or SH (C group), basal diet with 5 g/kg SH (SH group), and basal diet with antibiotics (ATB group). The antibiotic contents were 75 mg/kg aureomycin and 20 mg/kg kitasamycin. The composition and nutrient levels of the basal diet are shown in Table 1. On day 28, blood of eight pigs per treatment (two pigs per pen) was collected from the anterior vena cava using disposable syringes. Rectal fecal samples of ten pigs per treatment (two or three pigs per pen) were obtained. The sampling progress was performed by an experienced veterinary assistant, and no analgesia or anesthetic was given. None of the piglet died all through the experiment period. After the experiment was over, the piglets continued to be kept by Hangzhou Zhengxing Animal Husbandry co. LTD till they were marketed. Fecal samples were divided immediately into two aliquots; one aliquot was stored at −80 ◦C for microbial 16S rDNA sequencing analysis, and the other aliquot was stored on ice for plate count analysis of E. coli. Growth performance measurement The piglets were individually weighed on days 0, 14, and 28 of the experiment. Feed intake per pen was documented weekly, and the residual feed was measured at the end of the experiment. Average daily gain (ADG), average daily feed intake (ADFI), and feed intake to gain ratio (F/G) were calculated based on these parameters (n = 4, a pen was considered as an experimental unit).

Sun et al. (2020), PeerJ, DOI 10.7717/peerj.9067 3/18 Table 1 Composition and nutritional characteristics of the basal diet.

Items Content Ingredients (g/kg of diet) Corn 510 Extruded soybean 130 Soybean meal 180 Whey powder 100 Fish meal 50 Monocalcium phosphate 8 Limestone 5 Salt 3 Choline chloride 1 L-lysine·HCl 2 DL-methionine 0.8 L-threonine 0.8 Vitamin and medicine Premixa 4.4 Trace mineral Premixb 5 Analytical composition (g/kg of DM) Crude protein 200 Digestible energy (MJ/kg) 142 Crude fiber 28.3 Crude fat 49.6 Digestible lysine 11.4 Digestible methionine 3.3 Digestible threonine 7.4 Digestible tryptophan 2.2 Calcium 7.5 Total phosphorus 6.6

Notes. a Provided per kg of complete diet: 7,500 IU vitamin A; 750 IU vitamin D3; 25 IU vitamin E; 2.0 mg vitamin K3; 1.875 mg vitamin B1; 3.75 mg vitamin B2; 2.19 mg vitamin B6; 0.025 mg vitamin B12; 25 mg niacin; 15.6 mg D-pantothenic acid; 2.0 mg folic acid; 0.1875 mg biotin; 100 g phytase. b Provided per kg of complete diet: 25 mg Cu (as CuSO4·5H2O); 100 mg Zn (as ZnSO4); 30 mg Mn (as MnO2); 100 mg Fe (as FeSO4·H2O); 0.3 mg Se (as Na2SeO3·5H2O); 0.4 mg I (as Ca(IO3)2). Assay of immunological parameters in serum Blood samples (n = 8 per group, two pigs per pen) were centrifuged at speed of 3,500 rpm for 10 min to obtain serum. The concentrations of immunoglobulin G (IgG), interleukin- 1β (IL-1β), tumor necrosis factor (TNF)-α and myeloperoxidase (MPO) in serum were assessed using commercially available enzyme-linked immunosorbent assay (ELISA) kits (R&D Systems, Minneapolis, MN, USA) according to the manufacturer’s instructions. The colorimetric reaction was read in an automated ELISA microplate reader (Versamax, Molecular Devices). Viable plate counts of E. coli Rectal fecal samples of ten pigs per treatment (two or three pigs per pen) were obtained and feces from two or three pigs in the same pen were mixed into one sample. The mixed fecal

Sun et al. (2020), PeerJ, DOI 10.7717/peerj.9067 4/18 samples (n = 4 per group) were serially diluted (10−1–10−7) in sterilized saline solution. An aliquot of 100 µL of the sample was plated onto MacConkey agar plates and spread evenly by using an L-shaped spreader. Three parallel plates were prepared for each sample dilution. The plates were then inverted and incubated at 37 ◦C for 24 h. The number of colonies in the plates with 30–300 available isolated colonies was used to calculate E. coli population in feces. The calculated equation is as follows: Viable E. coli population in feces, colony-forming unit (CFU)/g = Number of E. coli colonies on the plate × dilution ratio of fecal sample/fecal weight. Microbiota analysis of fecal samples via 16S rRNA gene sequencing Microbial genome DNA of fecal samples (n = 10 per group, two or three pigs per pen) was isolated and purified using the QIAamp DNA Stool Mini Kit (Qiagen, GmbH Hilden, Germany) in accordance with the manufacturer’s instructions. The V3-V4 hypervariable regions of the 16S rRNA genes were PCR amplified from the microbial genomic DNA by using primers B341F–B785R (B341F: CCTACGGGNGGCWGCAG, B785R: GACTACHVGGGTATCTAATCC). PCR was performed in 25 µL of the reaction mixture with 12.5 µL of 2 × KAPA HiFi HotStart Ready Mix (KAPA Biosystems), 0.25 µL of 25 µM forward and reverse primers, and approximately 10 ng of template DNA. Thermal cycling involved initial denaturation at 95 ◦C for 3 min, followed by 25 cycles of denaturation at 95 ◦C for 30 s, annealing at 55 ◦C for 30 s, and elongation at 72 ◦C for 30 s and 72 ◦C for 5 min. The resulting amplicons were gel purified, quantified, pooled, and sequenced. Sequencing libraries were generated using a NEB Next R UltraTM DNA Library Prep Kit for Illumina (NEB, USA) in accordance with the manufacturer’s recommendations. The quality of the library was assessed with a Qubit@ 2.0 Fluorometer (Thermo Scientific) and an Agilent Bioanalyzer 2100 System (Agilent Technologies, Inc.). The library was sequenced on an Illumina Miseq platform, and 2 × 300 bp paired end reads were generated. Raw sequence reads were filtered and assembled. Sequences with contaminated adapters, undetermined nucleotide, or low complexity were removed. The resulting sequences were clustered into operational taxonomic units (OTUs) by using USEARCH drive 7 at 97% sequence similarity. Chimeric OTUs were removed with UCHIME v4.2. Representative sequences for each OTU were picked and aligned using QIIME 1.8. The Ribosomal Database Project Classifier v2.2 was used to assign a taxonomic rank to each sequence in the representative set. The relative abundance of each OTU was examined at different taxonomic levels. Genetic diversity calculation and taxonomic community assessment were performed with QIIME 1.8 scripts. Sequencing and bioinformatics analyses were conducted by Hangzhou KAITAI Biotechnology Co., Ltd. (Hangzhou, China). Statistical analysis Data were expressed as means or means ± SEM. Significant differences in growth parameters, immunological parameters, viable plate counts of E. coli, and the relative abundance of the genus were analyzed by one-way ANOVA followed by LSD post hoc test by using SPSS 12.0 (Chicago, USA) and the significance was considered at P < 0.05.

Sun et al. (2020), PeerJ, DOI 10.7717/peerj.9067 5/18 Table 2 Effect of Phellinus gilvus mycelium (SH) and antibiotic growth promoter (ATB) on the growth parameters in piglets.

Item Treatment SEM P-Value C ATB SH 1–14 days 191 ± 12.31 228 ± 7.64 207 ± 9.09 6.85 0.077 ADG 15–28 days 207 ± 16.78a 252 ± 18.89ab 277 ± 10.51b 12.0 0.033 1–28 days 199 ± 9.03a 240 ± 8.02b 242 ± 9.79b 7.57 0.013 1–14 days 309 ± 7.07 305 ± 20.90 315 ± 15.31 8.18 0.913 ADFI 15–28 days 463 ± 34.55 556 ± 9.21 517 ± 23.75 17.24 0.076 1–28 days 386 ± 18.95 430 ± 14.09 416 ± 19.23 10.73 0.246 1–14 days 1.63 ± 0.12 1.34 ± 0.09 1.52 ± 0.06 0.060 0.127 F/G 15–28 days 2.27 ± 0.16 2.23 ± 0.12 1.87 ± 0.06 0.084 0.088 1–28 days 1.95 ± 0.09 1.80 ± 0.02 1.72 ± 0.06 0.045 0.100

Notes. ADG, average daily gain; ADFI, average daily feed intake; F/G, feed intake to gain ratio; C, control. n = 4 (a pen was considered as an experimental unit; six pigs per pen); data are shown as means ± SEM. a,bvalues with different superscripts in the same row differ significantly (P < 0.05). For phylotype analysis, the alpha diversity of the microbiome was calculated on the basis of the OTU level by using USEARCH 7.0. Principal coordinate analysis (PCoA) was performed using R and visualized with the R package ggplot2, and significant differences were evaluated by Adonis analysis (R package vegan) at P < 0.05. Comparison of OTU levels between groups were assessed using the edgeR test in R by using the Benjamini and Hochberg false discovery rate, and the significance was considered at P < 0.05 and FDR < 0.2.

RESULTS Growth parameters The ADG of the ATB group and SH group in the entire stage (1–28 days) increased significantly (P < 0.05) compared with that of the control group (Table 2). SH treatment increased the ADG greatly at the later stage (15–28 days). The ADFI and F/G throughout the entire experimental period were not significantly changed in ATB or SH group compared with those in control group (P > 0.05). Immunological parameters We quantified the IgG, the important antibody in adaptive immunity, TNF-α and IL-1β, cytokines secreted mainly by monocyte-macrophages, and MPO, one biomarker of active neutrophil in serum. Results (Fig. 1A) show that IgG levels did not varied among groups, suggesting that ATB and SH did not affected the adaptive immunity. However, the levels of TNF- α, IL-1β and MPO were both increased by treatment of ATB or SH (Figs. 1B–1D), and these cytokine levels in SH group were significant higher than in ATB group (P < 0.05). These results indicated the better innate immune response of pigs in SH group than that of the control group and ATB group.

Sun et al. (2020), PeerJ, DOI 10.7717/peerj.9067 6/18 Figure 1 Serum immunological parameters in different treatment groups. (A) Immunoglobulin G (IgG); (B) myeloperoxidase (MPO); (C) interleukin 1 beta (IL-1β); (D) tumor necroses factor alpha (TNF-α). n = 8. Data are shown as means ± SEM. *P < 0.05. Full-size DOI: 10.7717/peerj.9067/fig-1

Viable E. coli counts in feces E. coli is a group opportunistic pathogens that may cause diarrhea in piglets. Figure 2 shows that both ATB and SH treatments decreased the viable E. coli counts in feces. Fecal microbiota structure analysis To further explore the influence of SH and ATB on the gut microbiota, we analyzed the structure of the fecal microbiota by 16S rRNA pyrosequencing. The diversity of the fecal microbes as displayed by the Richness, Chao1, Shannon, and Simpson indices (Figs. 3A–3D) was not significantly changed by SH or ATB treatment (P > 0.05). As displayed by PCoA on the OTU level (Fig. 3E), the microbiota of the SH group largely overlapped with the control. The ATB group was distinct from the control group in terms of position (P < 0.05), suggesting the significant ATB-induced change in the gut microbiota structure.

Sun et al. (2020), PeerJ, DOI 10.7717/peerj.9067 7/18 Figure 2 Effect of Phellinus gilvus. mycelium (SH) and antibiotic growth promoter (ATB) on viable Es- cherichia coli counts in piglets’feces. n = 4; *P < 0.05; n.s., no significant difference (P > 0.05). Full-size DOI: 10.7717/peerj.9067/fig-2

We also compared the relative abundance of each OTU in the SH and ATB groups with those in control group (Fig. 4). It shows that there were 271 OTUs significantly different in relative abundance between ATB group and control group; of these OTUs, 135 OTUs were significantly higher in relative abundance in ATB group than the control, and 136 OTUs were significantly lower in relative abundance in ATB group compared with the control. There were 68 OTUs significantly different in relative abundance between SH group and control group; of these OTUs, 30 OTUs were significantly higher in relative abundance in SH group than the control group, and 38 OTUs were significantly lower in relative abundance in SH group compared with the control. Figure 5 displays the changes in the relative abundance of the top 10 phyla, families, and genera. SH treatment slightly influenced the top 10 phyla, families, and genera compared with the control group. By contrast, ATB remarkably changed the structures of families and genera compared with the control group. Figure 6 shows the genera that were significantly altered in relative abundances by SH or ATB treatment compared with the control. SH treatment increased the relative abundance of Alloprevotella (P < 0.05). ATB treatment increased the abundance of Prevotella, Megasphaera and Faecalibacterium significantly (P < 0.05).

DISCUSSION As a result of the restriction of antibiotic growth promoters in feed, search for alternatives to antibiotics has become a hotspot. In the last decade, there has been a noticeable growth in interest in the potential of mushrooms and their application in animal feed. The growth promoting effect has been demonstrated in many mushroom strains in Basidiomycota taxon such as Agaricus bisporus, Hericium caput-medusae (Bull.:Fr.) Pers and Lentinus edodes (Giannenas et al., 2010; Shang et al., 2015; Guo et al., 2004). It is reported that dietary inclusion of Agaricus bisporus mushroom at 20 g/kg improved growth performance,

Sun et al. (2020), PeerJ, DOI 10.7717/peerj.9067 8/18 Figure 3 The diversity and structure of the gut microbiota in different groups. (A–D) Diversity as esti- mated by the Richness, Chao 1, Shannon, and Simpson indices; (E) Principal coordinate analysis (PCoA) plots of microbial communities; n = 10. Full-size DOI: 10.7717/peerj.9067/fig-3

feed efficiency in broiler chickens (Giannenas et al., 2010). Lentinus edodes extract at dose of 5g/kg in feed showed similar efficiency to antibiotic apramycin in improving body weight gain of broiler chickens infected with avian Mycoplasma gallisepticum (Guo et al., 2004). Mushroom Phellinus is also a genus belonged to Basidiomycota. Although multiple pharmacological activities of Phellinus spp. have been reported in laboratory animals (Chen et al., 2016; Sun et al., 2018; Wang et al., 2019a; Wang et al., 2019b), its effect on livestock has not been reported yet. In the present study, dietary inclusion of 5 g/kg SH for 28 days significantly increased the ADG (1–28 days) of weaned piglets, and the efficiency was similar to ATB. This result indicated the potent growth promoting effect of SH. Moreover, SH was more potent than ATB in increasing serum IL-1β and TNF-α, cytokines that are mainly secreted by monocyte-macrophages, and MPO, a

Sun et al. (2020), PeerJ, DOI 10.7717/peerj.9067 9/18 Figure 4 Comparison of OTUsof piglets’ fecal microbiota sequences between control group and treatment groups. (A) ATB group vs. Control group, (B) SH group vs. Control group. Full-size DOI: 10.7717/peerj.9067/fig-4

Figure 5 Relative abundance of the top 10 phyla, families, and genera of fecal microbiota in different groups. (A) Accumulated abundance of the top 10 phyla; (B) accumulated abundance of the top 10 families; (C) accumulated abundance of the top 10 genera. Full-size DOI: 10.7717/peerj.9067/fig-5

heme-containing peroxidase plays important role in microbial killing in neutrophils. But the IgG level in serum was not affected by any treatment. Monocyte-macrophages and neutrophils are powerful effector cells of innate immune system. Their microbicidal capacity, phagocytosis, and secretion of cytokines such as IL-1β and TNF-α are enhanced when activated (Sun et al., 2017; Aratani, 2018). IgG, antibodies created and released by plasma B cell, are the most common type of antibody found in blood circulation which participate predominantly in the adaptive immune response (Gudelj, Lauc & Pezer, 2018). Our results indicated that SH had better stimulation effect on innate immunity than the adaptive immunity. The immunomodulation effect is frequently reported in mushrooms, and polysaccharides are deemed to be the major active compounds. Li et al. (2015) found that Ganoderma-lucidum polysaccharides significantly increased serum concentrations of IgG and IL-2 in finisher pigs. Dalloul et al. (2006) also reported that

Sun et al. (2020), PeerJ, DOI 10.7717/peerj.9067 10/18 Figure 6 Relative abundance of the genera significantly changedby SH or ATB. (A) Prevotella; (B) Megasphaera; (C) Faecalibacterium; (D) Alloprevotella; (E) unassigned genera; (F) other genera. n = 10. Data are shown as means means ± SEM. a,b different superscripts on bars mean significant difference between groups (P < 0.05). Full-size DOI: 10.7717/peerj.9067/fig-6

mushroom and mushroom-derived lectin enhance innate immunity in broiler chicken. ATB also increased MPO, IL-1β and TNF-α in our study. It was reported that the effects on immunity varied between different ATBs (Cheng et al., 2018). In the light of the different antimicrobial spectrums and immunomodulatory capacities of different antibiotics, it is possible that the immunomodulation of ATB is related to the modulation of specific bacteria. Bacterial metabolites and components such as short chain fatty acids (SCFA) and lipopolysaccharides have been proved to be effective immunomodulatory compounds (Inan et al., 2000; Bäckhed et al., 2001). For SH, the immunomodulatory effect might not fully depend on the microbiota, but also on some components such as polysaccharides, because polysaccharides in Phellinus spp. has been proved to directly activate immune cells in vitro (Suabjakyong et al., 2015; Liu et al., 2016; Wang et al., 2019a; Wang et al., 2019b). The gut microbiota is a complex community comprising more than 100 trillion microbes that reside in the gut of humans and animals, and it is demonstrated to be important for the health of their host (Bridgewater et al., 2017; Li et al., 2019; Sircana et al., 2019). Mushrooms are reported to have impact on gut microbiota. In research of Shang et al. (2015), the polysaccharides of Hericium caput-medusae (Bull.:Fr.) Pers (HFCP) increased the caecum lactobacilli count, bifidobacteria count, and propionic acid concentration in broiler chickens but decreased the caecum E. coli count linearly and quadratically as the HFCP levels increased. Guo et al. (2004) reported that Lentinus edodes extract and antibiotic apramycin showed different effects on cecal microbial populations: the antibiotic decreased the cecal bifidobacteria and lactobacilli counts, but Lentinus edodes extract increased them. Guo et al. (2004) also found that the higher doses of Lentinus edodes extract the chicken given, the higher body weight gain and total aerobe and anaerobe counts the chicken had. The effects of SH on microbiota was also investigated in this study. Firstly,

Sun et al. (2020), PeerJ, DOI 10.7717/peerj.9067 11/18 we tested viable E. coli counts in feces. E. coli is a group of facultative anaerobes in human and animal gut. Some E. coli serotypes, such as E. coli O157: H7, cause serious diarrhea in pigs (Xia et al., 2018). Antibiotics are often used to treat E. coli-induced diarrhea, and the resistance of E. coli to antibiotics is frequently reported (Hammerum et al., 2006). Our results showed that the viable E. coli counts in feces were dramatically decreased by SH treatment, which indicated the inhibition effect of SH on E. coli. Pervious study (Reis et al., 2014) reported that the methanolic extract of Phellinus linteus showed strong antibacterial activity against several common pathogens including E. coli. Phellinstatin, one polyphenolic compound in Phellinus spp. that can be extracted by alcohols, can strongly inhibit bacterial enoyl-ACP reductase and may be one major compound accounting for the antibacterial activity of Phellinus spp. (Cho et al., 2011). In the 16S rRNA pyrosequencing analysis, SH treatment did not greatly change the diversity of the microbiota. SH also affected less OTUs than ATB, indicating the milder effects of SH on the gut microbiota structure than those of ATB. SH treatment increased the relative abundance of Alloprevotella genus, a group of SCFA-producing bacteria, which mainly produces butyric acid and acetic acid by fermentation of dietary fibers or indigestible carbohydrates (Cheng et al., 2019). Many reports have demonstrated that polysaccharides can increase the Alloprevotella relative abundant in gut (Chen et al., 2019; Cheng et al., 2019). Fibers and polysaccharides are not hydrolyzed by digestive enzymes or absorbed in the upper part of the gastrointestinal tract. These ingredients therefore enter the large intestine and may serve as substrates for the endogenous colonic bacteria. The SH contains a high proportion of fibers and polysaccharides, and this may play a role in the increasing of Alloprevotella relative abundant. It should be noted that the 16S rRNA pyrosequencing analysis only displayed the relative abundant of the total bacteria, not the absolute population of the bacteria. Therefore, it cannot be ruled out the possibilities that SH increased or decreased the population of total bacteria. ATB treatment increased the abundance of Prevotella, Megasphaera and Faecalibacterium genera. Prevotella, Megasphaera and Faecalibacterium are all common members of the gut microbiota in humans and animals (Kim & Isaacson, 2015; Yue et al., 2019; Nuzum et al., 2020), of which Prevotella is a dominant genus with high abundance (Kim & Isaacson, 2015). Although Prevotella genus takes up a high proportion in the normal flora, its role in human and animal health is controversial, with both positive and negative associations. Some researchers report that Prevotella genus play important roles in the utilization of feed proteins (Xu & Gordon, 2003; Han et al., 2015). While in other reports, many Prevotella species are linked to inflammation (Bertelsen, Elborn & Schock, 2019; Fteita et al., 2018). Nevertheless, the consistent finding is that high ratio of species in Prevotella have natural antibiotic-resistant genes tetQ and ermF (Arzese, Tomasetig & Botta, 2000; Veloo et al., 2019). Therefore, we speculate that the great increase of Prevotella in relative abundance might attribute to their relative insensitivity to antibiotics compared to other bacteria. This sepeculation is consistent with the previous research about carbadox, a broad spectrum antibiotic, in which research carbadox increased the relative abundance of Prevotella in swine gut but did not change its absolute abundance (Looft et al., 2014).

Sun et al. (2020), PeerJ, DOI 10.7717/peerj.9067 12/18 CONCLUSIONS Our work demonstrated for the first time that SH could promote growth and activate innate immunity in piglets. Unlike ATB, which altered the microbiota structure drastically, SH slightly influenced the structure of microbiota but only decreased fecal viable Escherichia coli counts. Our finding suggested that SH could be an alternative to ATB in piglet feed.

ACKNOWLEDGEMENTS We thank Doctor Zhichao Wang from Hangzhou KAITAI Biotechnology 153 Co., Ltd. (Hangzhou, China) for his assistance in 16S rRNA pyrosequencing analysis.

ADDITIONAL INFORMATION AND DECLARATIONS

Funding This work was supported by the Foundation from Science and Technology Department of Zhejiang Province (2018C02003, LGN18C170005), the China postdoctoral foundation (2018M632509), and the Zhejiang postdoctoral foundation (20170123). There was no additional external funding received for this study. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Grant Disclosures The following grant information was disclosed by the authors: Foundation from Science and Technology Department of Zhejiang Province: 2018C02003, LGN18C170005. China postdoctoral foundation: 2018M632509. Zhejiang postdoctoral foundation: 20170123. Competing Interests Cheng Zhang is an employee of Hangzhou Zhengxing Animal Husbandry co. LTD. Author Contributions • Yuqing Sun conceived and designed the experiments, performed the experiments, analyzed the data, prepared figures and/or tables, authored or reviewed drafts of the paper, and approved the final draft. • Shi Zhong performed the experiments, analyzed the data, authored or reviewed drafts of the paper, and approved the final draft. • Bo Deng and Jinxi Huo performed the experiments, authored or reviewed drafts of the paper, and approved the final draft. • Qinsheng Jin, Jie Wu, Jianxun Zhu and Cheng Zhang performed the experiments, prepared figures and/or tables, and approved the final draft. • Yougui Li conceived and designed the experiments, analyzed the data, authored or reviewed drafts of the paper, and approved the final draft.

Sun et al. (2020), PeerJ, DOI 10.7717/peerj.9067 13/18 Animal Ethics The following information was supplied relating to ethical approvals (i.e., approving body and any reference numbers): Medical Ethics Committee of Zhejiang Academy of Agricultural Sciences approved this study (No.2017-050). DNA Deposition The following information was supplied regarding the deposition of DNA sequences: The raw data of 16s rDNA sequences are available at Sequence Read Archive (SRA) in NCBI: Group C, SAMN13885614 to SAMN13885623; Group ATB, SAMN13885624 to SAMN13885633; Group SH are from SAMN13885634 to SAMN13885643. Data Availability The following information was supplied regarding data availability: The raw data is available in the Supplemental Files. Supplemental Information Supplemental information for this article can be found online at http://dx.doi.org/10.7717/ peerj.9067#supplemental-information.

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